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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415709Generated: October 30, 2026

4-Methyl-3-nitrobenzoic acid → HCID 896862, compound

https://huagongshe.com/reaction/2415709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-3-nitrobenzoic acidHCID 7319—
ReactantOxalyl chlorideHCID 65578—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 896862HCID 896862—

Reaction Steps

Oxalyl chloride (4.8 ml) was added to a solution of 3-nitro-4-methylbenzoic acid (9.06 g) in methylene chloride (100 ml) and DMF (a few drops) and the reaction stirred at ambient temperature for 16 hours. The reaction mixture was evaporated and the residue was dissolved in methylene chloride (100 ml). 3,4-Dichlorobenzylamine (7.04 g), 4-dimethylaminopyridine (0.31 g) and triethylamine (13.9 ml) were added and the reaction mixture was stirred at ambient temperature for 16 hours. The mixture was washed with a saturated aqueous sodium bicarbonate solution, dried over magnesium sulphate and evaporated. The residue was purified by column chromatography using a 250:8:1 mixture of methylene chloride, methanol and a saturated aqueous ammonium chloride solution as eluent to give N-(3,4-dichlorobenzyl)4-methyl-3-nitrobenzamide as a solid (9.95 g); NMR Spectrum: (DMSOd6) 2.57 (s, 3H), 4.47 (d, 2H), 7.31 (m, 1H), 7.56 (m, 2H), 7.61 (d, 1H), 8.1 (m, 1H), 8.47 (d, 1H), 9.3 (t, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06821965B1
Source datasetuspto-grants-2004_11
ORD IDord-1e3b89d706814b29b16a039628901c7c
Source noteuspto-grants-2004_11